Conditions:
Disturbances in the amino acid neurotransmitter (AANt), gamma-amino butyric acid (GABA) function are hypothesized to contribute to the neurobiology of Major Depressive Disorder (MDD) and insomnia. The principal objective of this project is to use magnetic resonance spectroscopy (MRS) to provide the first in vivo characterization of cortical GABA levels in individuals with primary insomnia, and to determine whether subjects with MDD, achieving a partial response with selective serotonin reuptake inhibitor treatment but still experiencing significant residual symptoms including insomnia, have altered levels of this neurotransmitter. The investigators are also exploring the correlation between cortical AANt levels and abnormalities in sleep parameters in primary insomnia and as a residual symptom of major depression.
Dates: November 2007 -
Study Status: Recruiting
Ages Eligible: 25 Years - 55 Years
Gender Eligible: Both
This trial accepts healthy volunteers
Patient Sample.
- Healthy subjects without insomnia (Group A) (n=10)
- Subjects with primary insomnia (Group B) (n=20)
- Subjects with a history of major depressive disorder and currently in partial
remission but with residual insomnia (Group C) (n=20)
Inclusion Criteria for Primary Insomnia Subjects:
- Males or females between the ages of 25 and 55 years
- Clinical diagnosis of primary insomnia meeting DSM-IV criteria.
- Current insomnia ratings (current Sleep Onset Latency SOL > 30 minutes, Insomnia
Severity Index (ISI) > 14, total sleep time (TST) < 6.5 hrs/night).
- No lifetime history of psychopathology other than primary insomnia.
- No sleep disorders previously identified as related to other conditions including
sleep disordered breathing, restless leg syndrome, periodic limb movement disorder,
chronic pain, gastro-esophageal reflux disease, sleep paralysis, nocturnal seizures,
nocturia, enuresis; also narcolepsy and REM behavior disorders (assessed by clinical
interview and Harvard Center and Cognition Habitual Sleep Survey).
Inclusion Criteria for Depressed Subjects:
- Males or females between the ages of 25 and 55 years
- Clinical diagnosis of major depression meeting DSM-IV criteria in partial remission
(HDRS-8-17), confirmed after semi-structured interview with the SCID and HDRS.
- On monotherapy with a single SSRI medication for a period of at least 6-weeks.
- Remaining symptoms of insomnia (current Sleep Onset Latency (SOL) > 30 minutes,
Insomnia Severity Index (ISI) > 14, TST < 6.5 hrs/night).
- Participation is judged clinically appropriate by treatment team.
- No sleep disorders previously identified as related to other conditions including
sleep disordered breathing, restless leg syndrome, periodic limb movement disorder,
chronic pain, gastro-esophageal reflux disease, sleep paralysis, nocturnal seizures,
nocturia, enuresis; also narcolepsy and REM behavior disorders.
Inclusion Criteria for Healthy Control Subjects:
- Males or females between the ages of 25 and 55 years
- No lifetime history of psychopathology or insomnia (current SOL < 30mins, ISI < 4,
TST > 6.5 hrs)
- At low risk for depression (e.g., no first degree relative with child onset,
recurrent, psychotic or bipolar depression)
Exclusion Criteria for all Subjects:
- History of serious medical or neurological illness
- Signs of major medical or neurological illness on examination or as a result of
laboratory studies
- History of psychoactive substance and/or alcohol dependence or abuse in past
6-months.
- Current use of any psychoactive medication or substance (with the exception of
caffeine, as noted below, and the use of an SSRI in the depressed group), during the
two weeks prior to the initial scan.
- More than the caffeine-equivalent of 3 cups of coffee per day, or any regular (i.e.,
more than 1x/2 weeks) use of caffeine after 7pm.
- Use of benzodiazepines or olanzapine in past 3-months.
- Pregnant or nursing
- Any implanted metal devise or metal fragments
Sponsors:
First Received: October 1, 2008
Last Updated: Oct 08, 2009
Clinicaltrials.gov ID:
NCT00765752
Study HIC # 0707002830
Conditions:
Disturbances in the amino acid neurotransmitter (AANt), gamma-amino butyric acid (GABA) function are hypothesized to contribute to the neurobiology of Major Depressive Disorder (MDD) and insomnia. The principal objective of this project is to use magnetic resonance spectroscopy (MRS) to provide the first in vivo characterization of cortical GABA levels in individuals with primary insomnia, and to determine whether subjects with MDD, achieving a partial response with selective serotonin reuptake inhibitor treatment but still experiencing significant residual symptoms including insomnia, have altered levels of this neurotransmitter. The investigators are also exploring the correlation between cortical AANt levels and abnormalities in sleep parameters in primary insomnia and as a residual symptom of major depression.
Dates: November 2007 -
Study Status: Recruiting
Ages Eligible: 25 Years - 55 Years
Gender Eligible: Both
Patient Sample.
- Healthy subjects without insomnia (Group A) (n=10)
- Subjects with primary insomnia (Group B) (n=20)
- Subjects with a history of major depressive disorder and currently in partial
remission but with residual insomnia (Group C) (n=20)
Inclusion Criteria for Primary Insomnia Subjects:
- Males or females between the ages of 25 and 55 years
- Clinical diagnosis of primary insomnia meeting DSM-IV criteria.
- Current insomnia ratings (current Sleep Onset Latency SOL > 30 minutes, Insomnia
Severity Index (ISI) > 14, total sleep time (TST) < 6.5 hrs/night).
- No lifetime history of psychopathology other than primary insomnia.
- No sleep disorders previously identified as related to other conditions including
sleep disordered breathing, restless leg syndrome, periodic limb movement disorder,
chronic pain, gastro-esophageal reflux disease, sleep paralysis, nocturnal seizures,
nocturia, enuresis; also narcolepsy and REM behavior disorders (assessed by clinical
interview and Harvard Center and Cognition Habitual Sleep Survey).
Inclusion Criteria for Depressed Subjects:
- Males or females between the ages of 25 and 55 years
- Clinical diagnosis of major depression meeting DSM-IV criteria in partial remission
(HDRS-8-17), confirmed after semi-structured interview with the SCID and HDRS.
- On monotherapy with a single SSRI medication for a period of at least 6-weeks.
- Remaining symptoms of insomnia (current Sleep Onset Latency (SOL) > 30 minutes,
Insomnia Severity Index (ISI) > 14, TST < 6.5 hrs/night).
- Participation is judged clinically appropriate by treatment team.
- No sleep disorders previously identified as related to other conditions including
sleep disordered breathing, restless leg syndrome, periodic limb movement disorder,
chronic pain, gastro-esophageal reflux disease, sleep paralysis, nocturnal seizures,
nocturia, enuresis; also narcolepsy and REM behavior disorders.
Inclusion Criteria for Healthy Control Subjects:
- Males or females between the ages of 25 and 55 years
- No lifetime history of psychopathology or insomnia (current SOL < 30mins, ISI < 4,
TST > 6.5 hrs)
- At low risk for depression (e.g., no first degree relative with child onset,
recurrent, psychotic or bipolar depression)
Exclusion Criteria for all Subjects:
- History of serious medical or neurological illness
- Signs of major medical or neurological illness on examination or as a result of
laboratory studies
- History of psychoactive substance and/or alcohol dependence or abuse in past
6-months.
- Current use of any psychoactive medication or substance (with the exception of
caffeine, as noted below, and the use of an SSRI in the depressed group), during the
two weeks prior to the initial scan.
- More than the caffeine-equivalent of 3 cups of coffee per day, or any regular (i.e.,
more than 1x/2 weeks) use of caffeine after 7pm.
- Use of benzodiazepines or olanzapine in past 3-months.
- Pregnant or nursing
- Any implanted metal devise or metal fragments
Sponsors:
First Received: October 1, 2008
Last Updated: Oct 08, 2009
Clinicaltrials.gov ID:
NCT00765752
Study HIC # 0707002830
Donna K Fasula, APRN
203-764-9131
madonna.fasula@yale.edu
KristaJoy Altland, BS
203-764-9141
kristajoy.altland@yale.edu
Sanacora, Gerard
Principal Investigator
HIC # 0805003779
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